IL155937A0 - Imidazole and benzimidazole derivatives and pharmaceutical compositions containing the same - Google Patents
Imidazole and benzimidazole derivatives and pharmaceutical compositions containing the sameInfo
- Publication number
- IL155937A0 IL155937A0 IL15593701A IL15593701A IL155937A0 IL 155937 A0 IL155937 A0 IL 155937A0 IL 15593701 A IL15593701 A IL 15593701A IL 15593701 A IL15593701 A IL 15593701A IL 155937 A0 IL155937 A0 IL 155937A0
- Authority
- IL
- Israel
- Prior art keywords
- imidazole
- same
- pharmaceutical compositions
- compositions containing
- benzimidazole derivatives
- Prior art date
Links
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 title 3
- 229940058303 antinematodal benzimidazole derivative Drugs 0.000 title 1
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 title 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
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- C07D233/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
- C07K5/0202—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-X-X-C(=0)-, X being an optionally substituted carbon atom or a heteroatom, e.g. beta-amino acids
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
- C07K5/0205—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-(X)3-C(=0)-, e.g. statine or derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurology (AREA)
- Physical Education & Sports Medicine (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Oncology (AREA)
- Diabetes (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Communicable Diseases (AREA)
- Virology (AREA)
- Biochemistry (AREA)
- Genetics & Genomics (AREA)
- Immunology (AREA)
- Biophysics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Addiction (AREA)
- Psychiatry (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25225200P | 2000-11-21 | 2000-11-21 | |
| PCT/US2001/047688 WO2002042278A2 (en) | 2000-11-21 | 2001-11-19 | Imidazole and benzimidazole caspase inhibitors and uses thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL155937A0 true IL155937A0 (en) | 2003-12-23 |
Family
ID=22955229
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL15593701A IL155937A0 (en) | 2000-11-21 | 2001-11-19 | Imidazole and benzimidazole derivatives and pharmaceutical compositions containing the same |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US7205327B2 (en) |
| EP (1) | EP1341767B1 (en) |
| JP (2) | JP4349802B2 (en) |
| KR (1) | KR20040020042A (en) |
| CN (1) | CN1298707C (en) |
| AP (1) | AP2003002811A0 (en) |
| AT (1) | ATE359274T1 (en) |
| AU (1) | AU2002232541A1 (en) |
| BG (1) | BG107841A (en) |
| BR (1) | BR0115546A (en) |
| CA (1) | CA2429630A1 (en) |
| CO (1) | CO7250442A2 (en) |
| CZ (1) | CZ20031730A3 (en) |
| DE (1) | DE60127860T2 (en) |
| EA (1) | EA200300601A1 (en) |
| ES (1) | ES2283456T3 (en) |
| HR (1) | HRP20030494A2 (en) |
| HU (1) | HUP0301870A3 (en) |
| IL (1) | IL155937A0 (en) |
| IS (1) | IS6822A (en) |
| MX (1) | MXPA03004459A (en) |
| NO (1) | NO20032270L (en) |
| NZ (1) | NZ526420A (en) |
| PL (1) | PL362612A1 (en) |
| SK (1) | SK7792003A3 (en) |
| WO (1) | WO2002042278A2 (en) |
| ZA (1) | ZA200303895B (en) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20011350A1 (en) | 2000-05-19 | 2002-01-15 | Vertex Pharma | PROPHARMAC OF AN INHIBITOR OF INTERLEUKIN-1ß CONVERTER ENZYME (ICE) |
| AU2003211052A1 (en) * | 2002-02-11 | 2003-09-04 | Vertex Pharmaceuticals Incorporated | Phospholipids as caspase inhibitor prodrugs |
| EP1499898A2 (en) | 2002-04-19 | 2005-01-26 | Vertex Pharmaceuticals Incorporated | Regulation of tnf-alpha |
| US20060217299A1 (en) * | 2003-02-24 | 2006-09-28 | Hirofumi Doi | Degradation inhibitor for hepatitis b virus x interacting protein |
| AU2003902704A0 (en) * | 2003-05-29 | 2003-06-19 | Crc For Waste Management And Pollution Control Limited Of Unsw | Process for producing a nanoscale zero-valent metal |
| US7297714B2 (en) * | 2003-10-21 | 2007-11-20 | Irm Llc | Inhibitors of cathepsin S |
| AU2005249503B2 (en) | 2003-11-10 | 2011-08-25 | Vertex Pharmaceuticals Incorporated | ICE inhibitors for the treatment of autoinflammatory diseases |
| JP4898658B2 (en) * | 2004-03-12 | 2012-03-21 | バーテックス ファーマシューティカルズ インコーポレイテッド | Methods and intermediates for the preparation of aspartate acetal caspase inhibitors |
| CN102362867A (en) * | 2004-05-15 | 2012-02-29 | 沃泰克斯药物股份有限公司 | Treating seizures using ice inhibitors |
| PT1796660T (en) * | 2004-09-17 | 2017-02-13 | Biomas Ltd | Use of ammonium trichloro(dioxyethylene-o,o')tellurate (as101) for the inhibition of interleukin-1beta-converting enzyme |
| CA2616337A1 (en) * | 2005-07-28 | 2007-02-08 | Vertex Pharmaceuticals Incorporated | Caspase inhibitor prodrugs |
| EP2288615B1 (en) | 2008-05-21 | 2017-06-21 | Genesis Technologies Limited | Selective caspase inhibitors and uses thereof |
| PL2380881T3 (en) * | 2008-12-26 | 2017-07-31 | Sumitomo Dainippon Pharma Co., Ltd. | Novel bicyclic heterocyclic compound |
| US9045524B2 (en) | 2009-05-21 | 2015-06-02 | Novagenesis Foundation | Selective caspase inhibitors and uses thereof |
| WO2011094426A1 (en) | 2010-01-29 | 2011-08-04 | The United State Of America, As Represented By The Secretary, Department Of Health & Human Services | Caspase inhibitors |
| TWI402072B (en) | 2010-10-19 | 2013-07-21 | Lilly Co Eli | Cathepsin s inhibitor compounds |
| EP2635906A4 (en) | 2010-11-05 | 2014-04-02 | Univ Brandeis | ICE-INHIBITING COMPOUNDS AND ITS USES |
| WO2012140500A1 (en) | 2011-04-15 | 2012-10-18 | New World Laboratories, Inc. | Selective cysteine protease inhibitors and uses thereof |
| US9956260B1 (en) | 2011-07-22 | 2018-05-01 | The J. David Gladstone Institutes | Treatment of HIV-1 infection and AIDS |
| US9790188B2 (en) | 2013-03-15 | 2017-10-17 | Whitehead Institute For Biomedical Research | Benzimidazole derivatives and uses thereof |
| TWI764977B (en) | 2017-01-23 | 2022-05-21 | 大陸商正大天晴藥業集團股份有限公司 | Bicyclic compound as CASPASE inhibitor, pharmaceutical composition containing same and use thereof |
| MX2021000714A (en) * | 2018-07-19 | 2021-03-25 | Sumitomo Pharma Co Ltd | Medicinal preparation for external use. |
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|---|---|---|---|---|
| US5714484A (en) * | 1993-12-08 | 1998-02-03 | Prototek, Inc. | α-(1,3-dicarbonylenol ether) methyl ketones as cysteine protease inhibitors |
| US5716929A (en) * | 1994-06-17 | 1998-02-10 | Vertex Pharmaceuticals, Inc. | Inhibitors of interleukin-1β converting enzyme |
| NZ334605A (en) | 1996-09-12 | 2000-08-25 | Idun Pharmaceuticals Inc | C-terminal modified (n-substituted)-2-indolyl dipeptides as inhibitors of the ice/ced-3 family of cysteine proteases and for treatments of inflammatory, autoimmune, neurodegenerative disorders and in the prevention of ischemic injury |
| US20040192743A1 (en) * | 2003-02-12 | 2004-09-30 | Mjalli Adnan M.M. | Substituted azole derivatives as therapeutic agents |
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- 2001-11-19 BR BR0115546-6A patent/BR0115546A/en not_active IP Right Cessation
- 2001-11-19 AU AU2002232541A patent/AU2002232541A1/en not_active Abandoned
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